trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: apotex corp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler apotex corp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 300 mg/1

Manufacturer
Apotex Corp

Identifiers & Regulatory

Product NDC 60505-2659
Product ID 60505-2659_5510dc85-9967-d02e-80d0-7a7e8ae1af2a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071196
Listing Expiration 2026-12-31
Marketing Start 2009-01-05

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 605052659
Hyphenated Format 60505-2659

Supplemental Identifiers

RxCUI
856364 856369 856373 856377
UPC
0360505265411 0360505265312 0360505265510 0360505265916
UNII
6E8ZO8LRNM

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name trazodone hydrochloride (source: ndc)
Generic Name trazodone hydrochloride (source: ndc)
Application Number ANDA071196 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (60505-2659-1)
  • 500 TABLET in 1 BOTTLE (60505-2659-5)
  • 1400 TABLET in 1 BOTTLE (60505-2659-7)
source: ndc

Packages (3)

60505-2659-1 100 TABLET in 1 BOTTLE (60505-2659-1) 60505-2659-5 500 TABLET in 1 BOTTLE (60505-2659-5) 60505-2659-7 1400 TABLET in 1 BOTTLE (60505-2659-7)

Ingredients (1)

trazodone hydrochloride (300 mg/1)

Linked Drug Pages (1)

Trazodone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5510dc85-9967-d02e-80d0-7a7e8ae1af2a", "openfda": {"upc": ["0360505265411", "0360505265312", "0360505265510", "0360505265916"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856369", "856373", "856377"], "spl_set_id": ["71961ab1-951d-1493-f76c-2ff25cca2a85"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60505-2659-1)", "package_ndc": "60505-2659-1", "marketing_start_date": "20090105"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (60505-2659-5)", "package_ndc": "60505-2659-5", "marketing_start_date": "20090105"}, {"sample": false, "description": "1400 TABLET in 1 BOTTLE (60505-2659-7)", "package_ndc": "60505-2659-7", "marketing_start_date": "20090105"}], "brand_name": "Trazodone Hydrochloride", "product_id": "60505-2659_5510dc85-9967-d02e-80d0-7a7e8ae1af2a", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "60505-2659", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA071196", "marketing_category": "ANDA", "marketing_start_date": "20090105", "listing_expiration_date": "20261231"}